# FDA Inspection 1282240 - Unilever Manufacturing (US), Inc. - September 15, 2025

Source: https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/3d172843-ae58-4695-8959-02871d2bad7a
Source feed: FDA_Inspections

> FDA Inspection 1282240 for Unilever Manufacturing (US), Inc. on September 15, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1282240
- Company Name: Unilever Manufacturing (US), Inc.
- Inspection Date: 2025-09-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Office Name: Dallas District Office

## Related Documents

- [FDA Inspection 1120502 - 2020-03-10](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/ed7479d8-73a2-4317-a645-7ca906399315)
- [FDA Inspection 942794 - 2015-07-10](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/b3a34659-cdfc-4f25-9943-2102334846aa)

Company: https://www.keypedia.com/companies/unilever-manufacturing-us-inc/ae587d51-1cf8-4ced-af22-8da0d2758cf6

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9